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Roux-en-Y Gastric Bypass (RYGB) Versus Omega-Loop Gastric Bypass (OLGB) Safety and Efficacy Short-term Study (ROSESS)

Primary Purpose

Obesity, Severe, Diabetes Mellitus, Type 2

Status
Unknown status
Phase
Not Applicable
Locations
Czech Republic
Study Type
Interventional
Intervention
Roux-en-Y Gastric Bypass
Omega-Loop Gastric Bypass
Sponsored by
Nemocnice Břeclav, p.o.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obesity, Severe focused on measuring Roux-en-Y Gastric Bypass, Omega-Loop Gastric Bypass, "Mini-Gastric" Bypass

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Severe Obesity: BMI ≥ 40 and ≤ 50 or (BMI ≥ 35 and < 40 and type 2 diabetes or metabolic syndrome)
  • Inadequate results of Attempts to loose weight by Conservative means
  • Ability to understand the nature of the procedure and willing to follow postoperative routine lifestyle and checkups
  • no contraindication for bariatric surgery on psychological assessment
  • no contraindication for general anesthesia
  • consent for both variants of gastric bypass surgery
  • consent to participate in a study with randomized design

Exclusion Criteria:

  • prior bariatric surgery of any kind
  • gravidity or recent (<1 year) labour
  • drug or alcohol abuse
  • symptomatic Gastro Esophageal Reflux Disease (GERD)
  • hiatal hernia, > 3cm
  • esophagitis, ≥ 2. grade
  • active smoker
  • chronic renal disease, stage ≥ 3
  • patient immobility
  • surgery not covered by universal insurance in Czech rep. (i.e. international patients)

Sites / Locations

  • Bariatric Clinic, Breclav Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Roux-en-Y Gastric Bypass

Omega-Loop Gastric Bypass

Arm Description

Laparoscopic Roux-en-Y Gastric Bypass and routine care.

Laparoscopic Omega-Loop Gastric Bypass and routine care.

Outcomes

Primary Outcome Measures

Composite measure of success of bariatric surgery as measured by Bariatric Analysis and Reporting Outcome System (BAROS)
BAROS composite score rates weight loss, change in comorbidities, and quality of life.

Secondary Outcome Measures

Change in weight, measured as Percent of Excess Weight Loss (%EWL)
Change in weight, measured as Percent of Excess Body Mass Index Loss (%EBMIL)
Change in Type 2 Diabetes Mellitus, measured as intensity of medical treatment: increased, same, decreased, or discontinued
Change in Type 2 Diabetes Mellitus, measured as intensity of treatment: diet alone, oral antidiabetic agent(s), insulin (IU/day)
Durability of change in Type 2 Diabetes Mellitus, measured as proportion of patients with T2DM partial remission who experience T2DM "relapse"
Change in Hypertension, measured as intensity of medical treatment: increased, same, decreased, or discontinued
Change in Dyslipidemia, measured as intensity of medical treatment: increased, same, decreased, or discontinued
Change in Obstructive Sleep Apnea (OSA), measured as the need of use of mouth device
Change in Obstructive Sleep Apnea, measured as score on Epworth questionnaire scale
Incidence of Ulcer or other Abnormal Finding on Endoscopic Gastroscopy, measured as proportion of patients with abnormal finding in each arm
Incidence of Ulcer or other Abnormal Finding on Endoscopic Gastroscopy, measured as Rate of unique Event per 100 patient-years of follow up
Incidence of early postoperative (<=30 days) Reoperations and Complications of grade >= 2 according to Clavien-Dindo classification
Incidence of late (>30 days) Reoperations, Complications, and detected adverse outcomes
Incidence of Reoperations, Complications, and detected adverse outcomes, measured as Rate of Event per 100 patient-years of follow up
Change in Quality of Life, as measured by Moorehead-Ardelt Questionnaire II

Full Information

First Posted
October 31, 2014
Last Updated
November 10, 2014
Sponsor
Nemocnice Břeclav, p.o.
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1. Study Identification

Unique Protocol Identification Number
NCT02290418
Brief Title
Roux-en-Y Gastric Bypass (RYGB) Versus Omega-Loop Gastric Bypass (OLGB) Safety and Efficacy Short-term Study
Acronym
ROSESS
Official Title
Prospective Randomized Controlled Clinical Study Comparing Two Bariatric Bypass Procedures, Roux-en-Y Gastric Bypass (RYGB) and Omega-Loop Gastric Bypass (OLGB), in Patients With Severe Obesity and Metabolic Disease
Study Type
Interventional

2. Study Status

Record Verification Date
November 2014
Overall Recruitment Status
Unknown status
Study Start Date
January 2012 (undefined)
Primary Completion Date
June 2016 (Anticipated)
Study Completion Date
December 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Nemocnice Břeclav, p.o.

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of this study is to compare the relative clinical outcomes between two variants of gastric bypass [Roux-en-Y Gastric Bypass (RYGB) or Omega-Loop Gastric Bypass (OLGB)] in metabolic surgery candidates with Body Mass Index (BMI) between 35 and 50. The study will examine the short and medium term effects of each intervention on weight, obesity comorbidities, quality of life and gastroscopy findings.
Detailed Description
Introduction: Obesity is a risk factor for Diabetes, Ischemic heart disease, Stroke, and Hypertensive heart disease, which are the 6th, 1st, 2nd, and 10th leading causes of death according to the WHO. Bariatric or Metabolic Surgery is an Efficient and reasonably Safe method for the Treatment of Severe Obesity, Type 2 Diabetes (T2DM) and Metabolic Syndrome (MS). Existing knowledge: Metabolic procedures, e.g. Gastric bypass, are more effective in the treatment of T2DM than predominantly "restrictive" procedures, e.g. Gastric Banding. RYGB is one of the most prevalent procedures in the world and Europe. In the USA, RYGB is considered a "golden standard" in bariatric surgery. In the recent decade, a simpler variant of Gastric bypass, i.e. OLGB, has been proposed. Proponents of OLGB argue it has less complications and seems to have higher and more durable effect on weight reduction and T2DM improvement. Opponents of OLGB are concerned that chronic exposure of gastric or esophageal mucosa to bile, as seen in animal experiments and in patients operated for gastric cancer or peptic ulcer disease, pose a severe health risk. So far, this concerns has not been confirmed in OLGB patients. Only one Randomized Controlled Trial (RCT) of these two interventions was performed, concluding OLGB to be simpler and safer with a similar Efficacy 2 years after the surgery. Need for a trial: A growing evidence supports the efficacy and safety of bariatric and metabolic surgery for the treatment of severe obesity and T2DM. Therefore, bariatric surgery is being more frequently performed. However, there is little evidence from randomized trials comparing different bariatric procedures - most comes from retrospective cohorts, which might suffer from bias. As a result, the choice of a bariatric procedure for a particular patient is based largely on the preference and experience of the particular surgeon, rather than evidence of best benefit for a particular patient. Although the efficacy and safety of RYGB is well established, newer variants or other less frequently employed bariatric procedures might offer more preferable Efficacy or Safety profile for some patients. Some evidence suggests OLGB might a promising procedure, which is "simpler and safer with similar efficacy" in comparison to RYGB, a technically more demanding procedure. This study contributes with rigorous evidence to further define the relative strengths and weaknesses of OLGB as compared to the "gold standard" RYGB. Objectives: The purpose of this study is to objectively compare the efficacy of RYGB and OLGB on weight, T2DM and other obesity-related comorbidities. Furthermore, this study aims to provide more insight into the safety of OLGB and RYGB by measuring the incidence of complications and abnormal findings on Gastroscopy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Severe, Diabetes Mellitus, Type 2
Keywords
Roux-en-Y Gastric Bypass, Omega-Loop Gastric Bypass, "Mini-Gastric" Bypass

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Roux-en-Y Gastric Bypass
Arm Type
Active Comparator
Arm Description
Laparoscopic Roux-en-Y Gastric Bypass and routine care.
Arm Title
Omega-Loop Gastric Bypass
Arm Type
Active Comparator
Arm Description
Laparoscopic Omega-Loop Gastric Bypass and routine care.
Intervention Type
Procedure
Intervention Name(s)
Roux-en-Y Gastric Bypass
Other Intervention Name(s)
RYGB
Intervention Description
Laparoscopic Gastric Bypass performed with two anastomoses (gastro-enteral and entero- enteral), two limbs (Alimentary limb of length 150cm and Biliary limb of length 75-100cm) and sewing of mesenteric defect.
Intervention Type
Procedure
Intervention Name(s)
Omega-Loop Gastric Bypass
Other Intervention Name(s)
OLGB, Mini-Gastric Bypass, Single Anastomosis Gastric Bypass
Intervention Description
Laparoscopic Gastric Bypass performed with single anastomosis (gastro-enteral) connecting a long gastric pouch to small bowel with Afferent limb of length 200cm.
Primary Outcome Measure Information:
Title
Composite measure of success of bariatric surgery as measured by Bariatric Analysis and Reporting Outcome System (BAROS)
Description
BAROS composite score rates weight loss, change in comorbidities, and quality of life.
Time Frame
baseline, 1 and 2 years
Secondary Outcome Measure Information:
Title
Change in weight, measured as Percent of Excess Weight Loss (%EWL)
Time Frame
baseline, 1 and 2 years
Title
Change in weight, measured as Percent of Excess Body Mass Index Loss (%EBMIL)
Time Frame
baseline, 1 and 2 years
Title
Change in Type 2 Diabetes Mellitus, measured as intensity of medical treatment: increased, same, decreased, or discontinued
Time Frame
baseline, 1 and 2 years
Title
Change in Type 2 Diabetes Mellitus, measured as intensity of treatment: diet alone, oral antidiabetic agent(s), insulin (IU/day)
Time Frame
baseline, 1 and 2 years
Title
Durability of change in Type 2 Diabetes Mellitus, measured as proportion of patients with T2DM partial remission who experience T2DM "relapse"
Time Frame
2 years
Title
Change in Hypertension, measured as intensity of medical treatment: increased, same, decreased, or discontinued
Time Frame
baseline, 1 and 2 years
Title
Change in Dyslipidemia, measured as intensity of medical treatment: increased, same, decreased, or discontinued
Time Frame
baseline, 1 and 2 years
Title
Change in Obstructive Sleep Apnea (OSA), measured as the need of use of mouth device
Time Frame
baseline, 1 and 2 years
Title
Change in Obstructive Sleep Apnea, measured as score on Epworth questionnaire scale
Time Frame
baseline, 1 and 2 years
Title
Incidence of Ulcer or other Abnormal Finding on Endoscopic Gastroscopy, measured as proportion of patients with abnormal finding in each arm
Time Frame
1 and 2 years
Title
Incidence of Ulcer or other Abnormal Finding on Endoscopic Gastroscopy, measured as Rate of unique Event per 100 patient-years of follow up
Time Frame
up to 5 years
Title
Incidence of early postoperative (<=30 days) Reoperations and Complications of grade >= 2 according to Clavien-Dindo classification
Time Frame
30 days
Title
Incidence of late (>30 days) Reoperations, Complications, and detected adverse outcomes
Time Frame
1 and 2 years
Title
Incidence of Reoperations, Complications, and detected adverse outcomes, measured as Rate of Event per 100 patient-years of follow up
Time Frame
up to 5 years
Title
Change in Quality of Life, as measured by Moorehead-Ardelt Questionnaire II
Time Frame
baseline, 1 and 2 years
Other Pre-specified Outcome Measures:
Title
Operative time, measured in minutes
Time Frame
intraoperative
Title
Length of inpatient stay due to performance of assigned intervention, measured in days
Description
number of days from the day of surgery (Post Operative Day 0) until the end of hospitalization
Time Frame
recorded at time of discharge, estimated average 4 days from the surgery
Title
Change in body weight, measured as proportion of patients with EWL > 50%, and proportion of patients with EWL < 25%
Time Frame
baseline, 1 and 2 years
Title
Change in body weight, measured in kilograms (kg)
Time Frame
baseline, 1 and 2 years
Title
Change in Body Mass Index (BMI), measured in kg/m2
Time Frame
baseline, 1 and 2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Severe Obesity: BMI ≥ 40 and ≤ 50 or (BMI ≥ 35 and < 40 and type 2 diabetes or metabolic syndrome) Inadequate results of Attempts to loose weight by Conservative means Ability to understand the nature of the procedure and willing to follow postoperative routine lifestyle and checkups no contraindication for bariatric surgery on psychological assessment no contraindication for general anesthesia consent for both variants of gastric bypass surgery consent to participate in a study with randomized design Exclusion Criteria: prior bariatric surgery of any kind gravidity or recent (<1 year) labour drug or alcohol abuse symptomatic Gastro Esophageal Reflux Disease (GERD) hiatal hernia, > 3cm esophagitis, ≥ 2. grade active smoker chronic renal disease, stage ≥ 3 patient immobility surgery not covered by universal insurance in Czech rep. (i.e. international patients)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michal Cierny, Dr.
Organizational Affiliation
Breclav Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Bariatric Clinic, Breclav Hospital
City
Breclav
ZIP/Postal Code
690 74
Country
Czech Republic

12. IPD Sharing Statement

Links:
URL
http://www.ncbi.nlm.nih.gov/pubmed/15973097?dopt=Abstract
Description
Laparoscopic Roux-en-Y versus mini-gastric bypass for the treatment of morbid obesity: a prospective randomized controlled clinical trial.
URL
http://link.springer.com/article/10.1007/s11695-012-0726-9
Description
Laparoscopic Roux-en-Y Vs. Mini-gastric Bypass for the Treatment of Morbid Obesity: a 10-Year Experience
URL
http://link.springer.com/article/10.1007/s11695-014-1180-7
Description
Greater Weight Loss with the Omega Loop Bypass Compared to the Roux-en-Y Gastric Bypass: a Comparative Study
URL
http://link.springer.com/article/10.1007/s11695-013-1026-8
Description
"Mini" Gastric Bypass: Systematic Review of a Controversial Procedure
URL
http://wlsr.eu
Description
Weight Loss Surgery Results
URL
http://www.ncbi.nlm.nih.gov/pubmed/24081459
Description
Interdisciplinary European guidelines on metabolic and bariatric surgery.

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Roux-en-Y Gastric Bypass (RYGB) Versus Omega-Loop Gastric Bypass (OLGB) Safety and Efficacy Short-term Study

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